Canonical Allele Identifier: CA377938218

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102830904-C-A
• MyVariant Identifiers: chr10:g.104590661C>A (hg19) ; chr10:g.102830904C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830904C>A , CM000672.2:g.102830904C>A	GRCh38
NC_000010.10:g.104590661C>A , CM000672.1:g.104590661C>A	GRCh37
NC_000010.9:g.104580651C>A	NCBI36
NG_007955.1:g.11630G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1325G>T (CYP17A1) MANE Select	ENSP00000358903.3:p.Cys442Phe
ENST00000638190.1:c.1022G>T (CYP17A1)	ENSP00000492539.1:p.Cys341Phe
ENST00000638272.1:c.869G>T (CYP17A1)	ENSP00000491508.1:p.Cys290Phe
ENST00000638971.1:c.1238G>T (CYP17A1)	ENSP00000492313.1:p.Cys413Phe
ENST00000639393.1:c.1328G>T (CYP17A1)	ENSP00000492651.1:p.Cys443Phe
ENST00000640633.1:n.1087G>T (CYP17A1)
ENST00000647664.1:c.*586C>A (WBP1L)	ENSP00000498131.1:n.*586C>A
ENST00000369887.3:c.1325G>T (CYP17A1)	ENSP00000358903.3:p.Cys442Phe
NM_000102.3:c.1325G>T (CYP17A1)	NP_000093.1:p.Cys442Phe
NM_000102.4:c.1325G>T (CYP17A1) MANE Select	NP_000093.1:p.Cys442Phe